Basic information Safety Supplier Related

3',4'-DIHYDROXYPROPIOPHENONE

Basic information Safety Supplier Related

3',4'-DIHYDROXYPROPIOPHENONE Basic information

Product Name:
3',4'-DIHYDROXYPROPIOPHENONE
Synonyms:
  • 1-(3,4-dihydroxyphenyl)-1-propanon
  • 3’,4’-dihydroxy-propiophenon
  • 3',4'-DIHYDROXYPROPIOPHENONE
  • 3,4-DIHYDROXYPROPIOPHENONE
  • 3',4'-Dihydroxypropiophenone,98%
  • 2-[3-(hydroxymethyl)phenoxy]acetic acid
  • 1-Propanone,1-(3,4-dihydroxyphenyl)-
  • 1-(3,4-dihydroxyphenyl)propan-1-one
CAS:
7451-98-1
MF:
C9H10O3
MW:
166.17
Product Categories:
  • Aromatic Propiophenones (substituted)
Mol File:
7451-98-1.mol
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3',4'-DIHYDROXYPROPIOPHENONE Chemical Properties

Melting point:
145-146°C
Boiling point:
375.1±27.0 °C(Predicted)
Density 
1.237±0.06 g/cm3(Predicted)
pka
8.75±0.31(Predicted)
CAS DataBase Reference
7451-98-1(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39

MSDS

  • Language:English Provider:ALFA
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3',4'-DIHYDROXYPROPIOPHENONE Usage And Synthesis

Uses

It is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.

Preparation

Obtained by Fries rearrangement of pyrocatechol dipropio-nate with aluminium chloride in chlorobenzene at 80° for 2 h (84%) or in nitrobenzene at 100° for 15 min;
Obtained by Fries rearrangement of pyrocatechol dipropionate with aluminium chloride in the presence of pyrocatechol, in nitrobenzene at 80° for 1 h (37%) or in nitromethane at r.t. for 72 h (76%)
Also obtained by Fries rearrangement of o-methoxyphenyl propionate (1 mol) by aluminium chloride (2 mol) without solvent at 140° for 2 h (51–55%) or in nitrobenzene at 80° for 30–60 min. A demethylation occurs during the reaction.
Also obtained by acylation of pyrocatechol with propionic acid
in the presence of boron trifluoride, at 150° for 2 h in a sealed tube ? (36%)
in the presence of polyphosphoric acid for 15 min in a boiling water bath ? (12%)
Preparation by demethylation of 4-hydroxy-3-methoxypropiophenone with refluxing pyridinium chloride for 10 min (80%)
Also obtained when propiovanillone was heated with an alkali sulfide under conditions used in the kraft cooking process.

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